Dichloromethane → HCID 75277253, compound

HRID 1429145Notes

Reaction equation

HRID 1429145 reaction equation
COC1C=CC(C[N:8]2[C:26](=[O:27])[N:25]3[CH:21]([CH2:22][CH:23]([O:28][C:29]4[CH:34]=[C:33]([O:35][CH3:36])[N:32]=[C:31]([C:37]5[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=5)[N:30]=4)[CH2:24]3)[C:20](=[O:43])[NH:19][C:18]3([C:44]([NH:46][S:47]([CH:50]4[CH2:52][CH2:51]4)(=[O:49])=[O:48])=[O:45])[CH:16]([CH2:17]3)[CH:15]=[CH:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]2)=CC=1.C(Cl)Cl.C([O-])(O)=O.[Na+]>C(O)(C(F)(F)F)=O>[CH3:36][O:35][C:33]1[N:32]=[C:31]([C:37]2[CH:38]=[CH:39][CH:40]=[CH:41][CH:42]=2)[N:30]=[C:29]([O:28][CH:23]2[CH2:22][CH:21]3[N:25]([C:26](=[O:27])[NH:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH:14]=[CH:15][CH:16]4[C:18]([C:44]([NH:46][S:47]([CH:50]5[CH2:52][CH2:51]5)(=[O:49])=[O:48])=[O:45])([NH:19][C:20]3=[O:43])[CH2:17]4)[CH2:24]2)[CH:34]=1

Participants

5

Procedure

Compound 6g was dissolved in a 1:2 mixture of TFA:DCM (24 ml) and stirred at RT for 1 h. NaHCO3 was added and the organic layer was separated of, dried, filtered and evaporated. The residue was purified by preparative HPLC which gave the pure title compound (19 mg, 8% over two steps), MS (M+H)+639.

Workup

  1. customthe organic layer was separated of,
  2. customdried
  3. filtrationfiltered
  4. customevaporated
  5. customThe residue was purified by preparative HPLC which

Sources & evidence

ORD record
ord-7ace2e1133564ba4935b981b67067850
Source dataset
uspto-grants-2015_01
Patent number
US08937080B2

Reaction notes

Loading…