HCID 14835022, compound → HCID 14835064, compound

HRID 728468Notes

Reaction equation

HRID 728468 reaction equation
[CH3:1][C:2]1[N:3]=[N:4][N:5]([CH:7]([CH3:32])[CH:8](N)[O:9][C:10](=[O:30])[NH:11][CH2:12][CH2:13][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][CH3:29])[N:6]=1.[Cl:33][CH2:34][CH2:35][CH2:36][S:37]([NH:40]CC(OC)CSCCCCCCCCCCCCCCCC)(=[O:39])=[O:38]>>[Cl:33][CH2:34][CH2:35][CH2:36][S:37]([NH:40][CH2:32][CH:7]([N:5]1[N:4]=[N:3][C:2]([CH3:1])=[N:6]1)[CH2:8][O:9][C:10](=[O:30])[NH:11][CH2:12][CH2:13][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][CH3:29])(=[O:39])=[O:38]

Participants

3

Procedure

2-(5-Methyl-2H-tetrazol-2-yl)-1-octadecylcarbamoyloxypropylamine IVh2 is allowed to react and worked up by the same procedure as described in (4). m.p. 70°-70.5° 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-4737fd52cff445b094e75f3d33d63fc8
Source dataset
uspto-grants-1991_09
Patent number
US05047540

Reaction notes

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