HCID 21247330, compound → HCID 14762990, compound

HRID 620522Notes

Reaction equation

HRID 620522 reaction equation
Cl.[CH3:2][C:3]([NH:7][CH2:8][C:9]1[C:22]2[C:23]3=[C:24]4[C:19](=[CH:20][CH:21]=2)[CH:18]=[CH:17][CH:16]=[C:15]4[CH:14]=[CH:13][C:12]3=[CH:11][CH:10]=1)([CH3:6])[CH2:4][OH:5]>CCO>[CH3:6][C:3]([NH:7][CH2:8][C:9]1[C:22]2[C:23]3=[C:24]4[C:19](=[CH:20][CH:21]=2)[CH:18]=[CH:17][CH:16]=[C:15]4[CH:14]=[CH:13][C:12]3=[CH:11][CH:10]=1)([CH3:2])[CH2:4][OH:5]

Participants

3

Reactant 1

HCID 21247330HCID 21247330, compound

Product 1

HCID 14762990HCID 14762990, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

Using the first part of the method in 1B, 2A gave 2-methyl-2((1-pyrenylmethyl)amino) propanol free base mp 135°-136°, (95% EtOH), (C, H, N).

Sources & evidence

ORD record
ord-853b395a7b1a463aa0509c9f12e62fb0
Source dataset
uspto-grants-1989_04
Patent number
US04820873

Reaction notes

Loading…