HCID 14835005, compound → HCID 14835061, compound

HRID 728464Notes

Reaction equation

HRID 728464 reaction equation
[CH3:1][C:2]1[N:6]([CH:7]([CH2:10][O:11][C:12](=[O:32])[NH:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31])[CH2:8][NH2:9])[N:5]=[N:4][N:3]=1.[Cl:33][CH2:34][CH2:35][CH2:36][S:37](NCC(OC)CSCCCCCCCCCCCCCCCC)(=[O:39])=[O:38]>>[Cl:33][CH2:34][CH2:35][CH2:36][S:37]([NH:9][CH2:8][CH:7]([N:6]1[C:2]([CH3:1])=[N:3][N:4]=[N:5]1)[CH2:10][O:11][C:12](=[O:32])[NH:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31])(=[O:39])=[O:38]

Participants

3

Procedure

2-(5-Methyl-1H-tetrazol-1-yl)-3-octadecylcarbamoyloxypropylamine IVi2 is allowed to react and worked up by the same procedure as described in (4). m.p. 74°-77° C. The summary of the experimental condition and the physical data of the product are listed in Table 7.

Workup

  1. customto react

Sources & evidence

ORD record
ord-e04e7b077fbf4b94be64209d4dd8b1cd
Source dataset
uspto-grants-1991_09
Patent number
US05047540

Reaction notes

Loading…