HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Diisopropylethylamine → N-{[(2S)-4-(3,4-dichlorobenzyl)morpholin-2-yl]methyl}-N'-[3-(pyrrolidin-1-ylsulfonyl)propyl]urea

HRID 1371459
Notes
Print preview

Reaction equation

HRID 1371459 reaction equation
[N:1]1([S:6]([CH2:9][CH2:10][CH2:11][NH2:12])(=[O:8])=[O:7])[CH2:5][CH2:4][CH2:3][CH2:2]1.C(N(CC)C(C)C)(C)C.[Cl:22][C:23]1[CH:24]=[C:25]([CH:47]=[CH:48][C:49]=1[Cl:50])[CH2:26][N:27]1[CH2:32][CH2:31][O:30][C@@H:29]([CH2:33][NH:34][C:35](=O)[O:36]C2C=CC([N+]([O-])=O)=CC=2)[CH2:28]1>CN(C)C=O.ClCCl>[Cl:22][C:23]1[CH:24]=[C:25]([CH:47]=[CH:48][C:49]=1[Cl:50])[CH2:26][N:27]1[CH2:32][CH2:31][O:30][C@@H:29]([CH2:33][NH:34][C:35]([NH:12][CH2:11][CH2:10][CH2:9][S:6]([N:1]2[CH2:2][CH2:3][CH2:4][CH2:5]2)(=[O:7])=[O:8])=[O:36])[CH2:28]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 81531DiisopropylethylamineHCID 117750244-Nitrophenyl [(2S)-4-(3,4-dichlorobenzyl)morpholin-2-yl]methylcarbamateHCID 133434513-(Pyrrolidine-1-sulfonyl)propan-1-amine

Product 1

HCID 69507245N-{[(2S)-4-(3,4-dichlorobenzyl)morpholin-2-yl]methyl}-N'-[3-(pyrrolidin-1-ylsulfonyl)propyl]ureaYield 63%

Reagents, catalysts & solvents 2

HCID 6228
Dimethylformamide
Solvent
HCID 6344DichloromethaneSolvent2×

Procedure

A solution of Intermediate 28 (0.027 g) in N,N-dimethylformamide (1 ml) and dichloromethane (2 ml) containing N,N-diisopropylethylamine (0.041 ml) was added to a stirred solution of Intermediate 13 (0.051 g) in dry dichloromethane (2 ml) at room temperature under nitrogen, and the mixture was stirred at room temperature for 21 h. The mixture was applied directly to a sulphonic acid ion exchange cartridge (2 g Isolute SCX) and eluted with methanol (6 column volumes) followed by 10% 880 ammonia in methanol (3 column volumes); evaporation of the methanol/ammonia fractions gave the crude product (0.063 g). Purification by chromatography on silica gel (2 g Varian Bond Elut cartridge), eluting with chloroform, ether, ethyl acetate, acetone, and methanol, gave the title compound as a gum (0.036 g).

Workup

  1. washeluted with methanol (6 column volumes)
  2. customevaporation of the methanol/ammonia fractions
  3. customgave the crude product (0.063 g)
  4. customPurification by chromatography on silica gel (2 g Varian Bond Elut cartridge)
  5. washeluting with chloroform, ether, ethyl acetate, acetone, and methanol

Sources & evidence

ORD record
ord-268a5bc8954942f9b4c0a1cd60369d0d
Source dataset
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07157457B2

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes